86883
Tetrabutylammonium nitrate
purum, ≥97.0% (NT)
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About This Item
Linear Formula:
(CH3CH2CH2CH2)4N(NO3)
CAS Number:
Molecular Weight:
304.47
EC Number:
217-726-0
UNSPSC Code:
12352116
PubChem Substance ID:
Beilstein/REAXYS Number:
3921016
MDL number:
InChI key
QHOKENWFMZXSEU-UHFFFAOYSA-N
InChI
1S/C16H36N.NO3/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;2-1(3)4/h5-16H2,1-4H3;/q+1;-1
SMILES string
[O-][N+]([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC
grade
purum
assay
≥97.0% (NT)
mp
116-118 °C (lit.), 116-120 °C
Other Notes
Recommended as supporting electrolyte in liquid ammonia; Synthesis of nitrates from triflates; used in the inversion of configuration of alcohols via tosylates; conversion of halides into ketones
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Ox. Sol. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
5.1B - Oxidizing hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
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N. Afza et al.
Zeitschrift fur Naturforschung, B: Chemical Sciences, 39, 840-840 (1984)
J.W. Zwikker et al.
Rec. Trav. Chim., 92, 581-581 (1973)
G. Cainelli et al.
Gazzetta Chimica Italiana, 116, 163-163 (1986)
G. Cainelli et al.
Tetrahedron Letters, 26, 3369-3369 (1985)
Fabio Galeotti et al.
Journal of chromatography. A, 1284, 141-147 (2013-03-05)
In this study, by using tetrabutylammonium bisulfate as ion-pairing reagent, we were able to separate all the main heparin/heparan sulfate disaccharides generated by the action of heparinases along with the main Hep tetrasaccharide possessing a 3-O-sulfate group on the sulfoglucosamine
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